ENZYMATICALLY SYNTHESIZED pH-RESPONSIVE IPN FOR IN-SITU RELEASE OF PANTOPRAZOLE SODIUM (Record no. 11183)

MARC details
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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200212103234.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200212b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12128
Author Sharma, Saruchi
245 ## - TITLE STATEMENT
Title ENZYMATICALLY SYNTHESIZED pH-RESPONSIVE IPN FOR IN-SITU RELEASE OF PANTOPRAZOLE SODIUM
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(4)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. Innovare Academic Sciences Pvt Ltd
Year 2019
300 ## - PHYSICAL DESCRIPTION
Pagination 98-103p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective: <br/>This study involves the synthesis of <br/>Gum tragacanth <br/>(gt) based interpenetrating polymer network (ipn) a<br/>nd its utilization for sustained <br/>release of anti-ulcerative drug i.e. pantoprazole s<br/>odium. <br/>Methods: <br/>IPN was synthesized from Gum tragacanth, polyacryli<br/>c acid (gt-cl-paa) hydrogel. gt-cl-paa was kept in <br/>distilled water. Further, acryamide <br/>(aam) and methylmethacrylate (mma) was added and th<br/>en kept for overnight. Later on, lipase and glutara<br/>ldehyde were added. Homopolymers and <br/>the unreacted monomers were removed using acetone. <br/>Synthesized IPN was dried at 50 °C for further stud<br/>y. <br/>Synthesized ipn was swelled in water and the drug w<br/>as added to it. The drug was entrapped in the pores<br/> of the synthesized ipn and then drug <br/>release behavior was studied using uv-vis spectroph<br/>otometer. <br/>Results: <br/>Gt, <br/>paa and mma based crosslinked IPN were synthesized <br/>using lipase-glutaraldehyde as initiator-crosslinke<br/>r system. The synthesized IPN <br/>was pH sensitive and possessed the desired swelling <br/>capacity required for the controlled and systematic<br/> liberation of pantoprazole sodium at 37 °C. <br/>The kinetic of drug release was studied and found t<br/>hat lateral diffusion (D<br/>L<br/>) of drug was higher as compared to the initial dif<br/>fusion (D<br/>I<br/>). The <br/>prepared IPN can be used as prospective carrier for<br/> prolonged drug delivery. <br/>Conclusion: <br/>A novel pH sensitive and colon targeted IPN was synt<br/>hesized. It acts as an effective device for the con<br/>trolled release of drug <br/>pantoprazole sodium.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 12129
Co-Author Vaneet Kumar
773 0# - HOST ITEM ENTRY
Title International journal of pharmacy and pharmaceutical science
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
International Standard Serial Number 2656-0097
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/31043/19676
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Articles Abstract Database
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Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 12/02/2020   2020916 12/02/2020 12/02/2020 Articles Abstract Database
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